“…Furthermore, compounds that contain azomethines are reactive intermediates for organic synthesis in different fields and have biological [7,8], anti-viral [9], anti-bacterial [10,11], and anti-fungal [12] effects, as well as inhibiting anti-microbial agents [13]. A search in the CCDC Database survey gave few results containing adamantan-1-ylaminomethylbenzene fragment or 1,4-di(aminomethyl)benzene fragment [14][15][16][17][18][19][20]. Structures similar to the title compound are absent in the database.…”
The title compound was synthesized by 2:1 condensation between adamantan-1-ylamine and benzene-1,4- dicarbaldehyde in n-BuOH and produced a good yield 87% of new bis Schiff base. The compound skeleton was affirmed by FTIR, 1H NMR, LC-MS, and X-ray powder diffraction. The structure was solved by a parallel tempering process and refined by using Rietveld refinement. Two adamantan-1-ylimino groups are connected in the anti-positions to the planar central 1,4-dimethylbenzene group. All rings of the adamantyl group possess normal chair conformation.
“…Furthermore, compounds that contain azomethines are reactive intermediates for organic synthesis in different fields and have biological [7,8], anti-viral [9], anti-bacterial [10,11], and anti-fungal [12] effects, as well as inhibiting anti-microbial agents [13]. A search in the CCDC Database survey gave few results containing adamantan-1-ylaminomethylbenzene fragment or 1,4-di(aminomethyl)benzene fragment [14][15][16][17][18][19][20]. Structures similar to the title compound are absent in the database.…”
The title compound was synthesized by 2:1 condensation between adamantan-1-ylamine and benzene-1,4- dicarbaldehyde in n-BuOH and produced a good yield 87% of new bis Schiff base. The compound skeleton was affirmed by FTIR, 1H NMR, LC-MS, and X-ray powder diffraction. The structure was solved by a parallel tempering process and refined by using Rietveld refinement. Two adamantan-1-ylimino groups are connected in the anti-positions to the planar central 1,4-dimethylbenzene group. All rings of the adamantyl group possess normal chair conformation.
“…Thiosemicarbazones are a class of important Schiff-bases and have received considerable attention for many years because of their biological activities and coordination chemistry properties [3][4][5][6][7][8][9][10][11][12][13][14]. In order to search for new thiosemicarbazones, the title compound was synthesized and its crystal structure was determined.…”
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